SBIR/STTR Research Award

IMMUNOGENICITY TESTING OF A FULLY SYNTHETIC SUBUNIT VACCINE AGAINST INFLUENZA

Award identifier 326d6bdad881b0b2545bfbb7aaa45b7baa401fa441978758451a84a220fe773cAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$299,994

Program and phase

SBIR · Phase I

Award year

2007

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
MEDIVAS, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): A formidable challenge confronting clinical immunology is the development of synthetic vaccines that could offer advantages over traditional methods in safety, reliability and cost. Appropriate delivery of protein and peptide antigens to the immune system has proved to be a major technical hurdle. The search for tractable solutions to this problem has received significant impetus in recent years by the development of biodegradable polymers as delivery vehicles. In this grant, we introduce poly(ester amide) co-polymers as a valuable addition to the current armory of suitable delivery polymers and present supportive initial proof-of-concept experiments that demonstrate the use of these polymers as a component of a protective vaccine for influenza. Specifically, these polymer-protein vaccine formulations can be rapidly modified to match alterations in influenza strains. The recent emergence of more virulent strains and the potential for a pandemic make it important that all new vaccine candidates be developed and tested. The experiments proposed here will define the capacity of PEA polymers to deliver polypeptide viral antigens by measuring both T cell stimulation and antibody production in response to diminished protein dosage. We propose to test polymer-coupled hemagglutinin and nucleoprotein antigens derived from H1N1 influenza for optimized dosage and schedule for influenza protection in mice. (Aim 1). We will test the ability of the vaccine candidates to protect animals from other influenza strains in mouse challenge studies (Aim 2). Finally, we will prepare the optimized formulations in several forms to assess their stability to storage in order to best prepare large quantities to use for human trials.(Aim 3) Successful achievement of these aims will provide impetus for development of commercially viable influenza vaccines that are rapidly prepared, stable in storage, and facile to transport to remote locales.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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